心房颤动的研究药物:激动剂和兴奋剂、进展和期望。

IF 4.9 2区 医学 Q1 PHARMACOLOGY & PHARMACY Expert opinion on investigational drugs Pub Date : 2024-09-01 Epub Date: 2024-08-08 DOI:10.1080/13543784.2024.2388583
Ruben Casado-Arroyo, Marco Bernardi, Pierre Sabouret, Giuseppe Franculli, Juan Tamargo, Luigi Spadafora, Nicolas Lellouche, Giuseppe Biondi-Zoccai, Peter P Toth, Maciej Banach
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引用次数: 0

摘要

简介心房颤动(房颤)是最常见的心律失常类型。由于全球人口老龄化和相关风险因素的增加,房颤的发病率也随之增加。最近,我们对心房颤动病理生理学的认识取得了进展,并确定了参与心房颤动促进心房重塑的结节参与者,这为新的治疗方法提供了潜在的机会:这篇详细的综述总结了房颤领域抗心律失常药物的最新进展:目前的情况远非最佳。尽管心房颤动治疗领域的药物开发有明确的未满足需求,但目前新药的开发还处于空白状态。该领域的一个限制因素是需要一种短期和长期无心脏和非心脏毒性的分子。提高对房颤遗传学、病理生理学、分子改变、大数据和人工智能的认识,以提供个性化的房颤治疗,将是未来几年房颤治疗的基石。
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Investigative agents for atrial fibrillation: agonists and stimulants, progress and expectations.

Introduction: Atrial fibrillation (AF) is the most common type of cardiac arrhythmia. Its prevalence has increased due to worldwide populations that are aging in combination with the growing incidence of risk factors associated. Recent advances in our understanding of AF pathophysiology and the identification of nodal players involved in AF-promoting atrial remodeling highlights potential opportunities for new therapeutic approaches.

Areas covered: This detailed review summarizes recent developments in the field antiarrhythmic drugs in the field AF.

Expert opinion: The current situation is far than optimal. Despite clear unmet needs in drug development in the field of AF treatment, the current development of new drugs is absent. The need for a molecule with absence of cardiac and non-cardiac toxicity in the short and long term is a limitation in the field. Improvement in the understanding of AF genetics, pathophysiology, molecular alterations, big data and artificial intelligence with the objective to provide a personalized AF treatment will be the cornerstone of AF treatment in the coming years.

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来源期刊
CiteScore
10.00
自引率
0.00%
发文量
71
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Investigational Drugs (ISSN 1354-3784 [print], 1744-7658 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on drugs in preclinical and early stage clinical development, providing expert opinion on the scope for future development. The Editors welcome: Reviews covering preclinical through to Phase II data on drugs or drug classes for specific indications, and their potential impact on future treatment strategies Drug Evaluations reviewing the clinical and pharmacological data on a particular drug Original Research papers reporting the results of clinical investigations on agents that are in Phase I and II clinical trials The audience consists of scientists, managers and decision-makers in the pharmaceutical industry, and others closely involved in R&D.
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